1. Home
  2. 2-[4-(4-fluorophenyl)phenyl]ethanamine;hydrochloride

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-[4-(4-fluorophenyl)phenyl]ethanamine;hydrochloride

NCCc1ccc(cc1)c1ccc(cc1)F.Cl Request for Quotation
Chemical Name: 2-[4-(4-fluorophenyl)phenyl]ethanamine;hydrochloride
CAS Number: 1189922-22-2
Product Number: AG0096II(AGN-PC-01LQPV)
Synonyms:
MDL No:
Molecular Formula: C14H15ClFN
Molecular Weight: 251.7270032

Identification/Properties

Computed Properties
Molecular Weight:
251.729g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
251.088g/mol
Monoisotopic Mass:
251.088g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
191
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-(4'-fluorobiphenyl-4-yl)ethanamine hydrochloride is a versatile compound widely used in chemical synthesis as a key building block for various organic molecules. Due to its unique structure and reactivity, this compound plays a crucial role in the creation of complex organic substances with specific properties and functionalities.In organic synthesis, 2-(4'-fluorobiphenyl-4-yl)ethanamine hydrochloride is often utilized as a precursor for the formation of biologically active compounds, pharmaceutical intermediates, and specialty chemicals. Its ability to serve as a nucleophilic amine group allows for the facile introduction of diverse functional groups, making it a valuable tool for synthetic chemists in designing and developing new molecules.Furthermore, the presence of the fluorine substituent in the biphenyl moiety confers additional properties to the resulting compounds, such as altered electronic properties, increased lipophilicity, and enhanced biological activity. This versatility makes 2-(4'-fluorobiphenyl-4-yl)ethanamine hydrochloride a valuable component in the synthesis of various target molecules for applications in medicinal chemistry, material science, and chemical biology.Overall, the application of 2-(4'-fluorobiphenyl-4-yl)ethanamine hydrochloride in chemical synthesis provides researchers with a powerful tool to access novel organic compounds with tailored properties and functions, contributing to the advancement of science and technology in diverse fields.